Resumen:
A novel class of thermostable G0 and G1-dendrimers was synthesized from the coupling of both propargyl
and azido esters derived from EDTA through copper catalyzed azide-alkyne cycloaddition. The branching
and size in these compounds were controlled by a simple azide-alkyne group position change in the
CuAAC reaction in conjunction with the use of 1,3-diazido-propan-2-ol as a polyfunctional compound.